Canonical Allele Identifier: CA2317591464

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1223017_1223020delinsCACC , CM000681.2:g.1223017_1223020delinsCACC	GRCh38
NC_000019.9:g.1223016_1223019delinsCACC , CM000681.1:g.1223016_1223019delinsCACC	GRCh37
NC_000019.8:g.1174016_1174019delinsCACC	NCBI36
NG_007460.2:g.38611_38614delinsCACC , LRG_319:g.38611_38614delinsCACC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.953_956delinsCACC	ENSP00000490268.2:p.Ala318=
ENST00000585748.3:c.581_584delinsCACC	ENSP00000477641.2:p.Ala194=
ENST00000585851.2:c.779_782delinsCACC	ENSP00000467912.2:p.Ala260=
ENST00000326873.12:c.953_956delinsCACC MANE Select	ENSP00000324856.6:p.Ala318=
ENST00000652231.1:c.953_956delinsCACC	ENSP00000498804.1:p.Ala318=
ENST00000326873.11:c.953_956delinsCACC	ENSP00000324856.6:p.Ala318=
ENST00000586243.5:c.953_956delinsCACC	ENSP00000467240.2:p.Ala318=
ENST00000589152.5:n.1651_1654delinsCACC
ENST00000591133.2:n.924_927delinsCACC
NM_000455.4:c.953_956delinsCACC , LRG_319t1:c.953_956delinsCACC	NP_000446.1:p.Ala318=
XM_005259617.1:c.953_956delinsCACC	XP_005259674.1:p.Ala318=
XM_005259618.3:c.953_956delinsCACC	XP_005259675.1:p.Ala318=
XM_011528209.1:c.731_734delinsCACC	XP_011526511.1:p.Ala244=
XR_936204.1:n.1729_1732delinsCACC
XM_005259617.3:c.953_956delinsCACC	XP_005259674.1:p.Ala318=
XM_011528209.2:c.731_734delinsCACC	XP_011526511.1:p.Ala244=
XR_001753738.2:n.1759_1762delinsCACC
XR_001753739.1:n.1759_1762delinsCACC
XR_001753740.2:n.1729_1732delinsCACC
NM_000455.5:c.953_956delinsCACC MANE Select	NP_000446.1:p.Ala318=